1. Visual Inspection
Each pump is examined for external damage, cracks, and signs of wear on the body and components. Cosmetic issues and potential safety concerns are noted for further action.
Alaris Medley Combo #2
In stock
$3,185.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Includes 1× Alaris 8015 PC Unit + 1× Alaris 8100 LVP Pump Module + 1× Alaris 8110 Syringe Module
- Two infusion modalities — large-volume and syringe infusion — managed through one PC Unit
- Guardrails Suite MX compatible • wireless-capable PC Unit • expandable modular Alaris platform
Alaris Medley Combo #2
Refurbished • 1-Year Warranty • Alaris 8015 PC Unit with one 8100 large-volume channel and one 8110 syringe-infusion channel
The Alaris Medley Combo #2 combines one Alaris 8015 PC Unit , one Alaris 8100 Pump Module , and one Alaris 8110 Syringe Module . The PC Unit provides the common system interface, while the 8100 delivers large-volume infusions and the 8110 provides syringe-based infusion capability. This combination gives facilities two different infusion modalities on the same modular Alaris platform.
What’s Included
- 1× CareFusion Alaris PC Unit, Model 8015 — system controller and programming interface
- 1× CareFusion Alaris Pump Module, Model 8100 — single-channel large-volume infusion module
- 1× CareFusion Alaris Syringe Module, Model 8110 — precision syringe infusion module
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, Alaris Medley Combo #2 combines large-volume and syringe infusion capabilities through a single Alaris 8015 PC Unit. The PC Unit supplies the common programming interface, power, and communications connection for both attached infusion modules.
The 8100 Pump Module supports continuous or intermittent large-volume delivery of fluids, medications, blood, and blood products. The 8110 Syringe Module provides continuous or intermittent syringe-based delivery for adult, pediatric, and neonatal patients. When used with an appropriately configured Alaris System, Guardrails Suite MX can apply facility-defined Profiles, Drug Library entries, dosing limits, and Clinical Advisories.
- One 8015 controller with one large-volume and one syringe-infusion channel
- 8100 flow rate: 0.1–999 mL/h • VTBI: 0.1–9999 mL
- 8110 flow rate: 0.01–999 mL/h depending on syringe size • approved syringe sizes span 1–60 mL
- Guardrails Suite MX compatible when an appropriate facility Data Set is installed
- Wireless-capable PC Unit; wireless functionality depends on installed hardware, software, network configuration, and facility settings
- Compatible administration sets, approved syringes, and appropriate facility configuration are required for clinical use
Specifications — Alaris 8015 PC Unit
| Manufacturer | CareFusion / BD |
| Model | 8015 — Alaris PC Unit |
| Type | System controller and common programming interface for compatible Alaris infusion and monitoring modules |
| Display | 4.7-inch diagonal display; display presentation may vary with facility Data Set and system configuration |
| Dimensions | 6.9″ W × 8.8″ H × 9″ D, including pole clamp |
| Weight | 7.2 lb |
| Module Capacity | Maximum of four infusion or monitoring modules; an Auto-ID Module may be included as a fifth module |
| Battery Operation | Battery runtime varies with module count and activity; manufacturer reference specifies approximately 6 hours with one Pump Module infusing at 25 mL/h using a new, fully charged battery |
| AC Power | 100–240 V AC, 50/60 Hz, 150 VA maximum |
| Communication Data Port | RS-232 with RJ45 connector |
| Safety Software | Compatible with Guardrails Suite MX; available Profiles, Drug Libraries, limits, and features depend on the installed facility Data Set and system configuration |
| Connectivity | Wireless-capable; wireless operation depends on installed hardware, software, network configuration, and facility settings |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–85% noncondensing for the 4.7-inch small-screen PC Unit |
| Software | Installed software version may vary by refurbished unit; verify the individual PC Unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8100 Pump Module
| Manufacturer | CareFusion / BD |
| Model | 8100 — Alaris Pump Module |
| Type | Single-channel large-volume infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Delivery | Continuous or intermittent infusion |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.6 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h |
| Flow-Rate Programming Increments | 0.1 mL/h from 0.1–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Volume to Be Infused (VTBI) | 0.1–9999 mL |
| VTBI Programming Increments | 0.01 mL from 0.1–9.99 mL; 0.1 mL from 10–999.9 mL; 1 mL from 1000–9999 mL |
| Rate Accuracy | ±5% at 1–999 mL/h and ±5.5% below 1 mL/h under manufacturer-specified test conditions |
| Occlusion — Pump Mode | 525 mmHg at rates of 30 mL/h or greater; threshold varies with rate and patient back-pressure below 30 mL/h |
| Occlusion — Selectable Mode | User-selectable from 50–525 mmHg in 25 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.1–20 mL/h in 0.1 mL/h increments |
| Air-in-Line Detection | Ultrasonic air-in-line detection |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8110 Syringe Module
| Manufacturer | CareFusion / BD |
| Model | 8110 — Alaris Syringe Module |
| Type | Syringe infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Administration Routes | Clinically acceptable routes including intravenous, intra-arterial, subcutaneous, epidural, enteral, and irrigation of fluid spaces |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D |
| Weight | 4.5 lb |
| Operating Principle | Positive displacement |
| Overall Flow Rate Range | 0.01–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.01–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Syringe-Specific Flow Ranges | 50/60 mL: 0.1–999 • 30 mL: 0.1–650 • 20 mL: 0.1–500 • 10 mL: 0.1–250 • 5 mL: 0.1–150 • 3 mL: 0.01–100 • 1 mL: 0.01–30 mL/h |
| Volume to Be Infused (VTBI) | 0.1–60 mL |
| Rate Accuracy | ±2% of full-scale plunger travel, excluding syringe variation |
| Syringe Compatibility | Approved syringe sizes span 1–60 mL. Compatible manufacturer and model combinations depend on installed Syringe Module software, country-specific compatibility documentation, and approved system configuration. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available selection list; the displayed syringe manufacturer/type and size must be verified before use |
| Maximum Infusion Pressure | Approximately 800 mmHg without pressure-sensing disc; 1060 mmHg with pressure-sensing disc |
| Occlusion Alarm Threshold | Without pressure-sensing disc: Low, Medium, or High; with pressure-sensing disc: user-selectable 25–1000 mmHg in 1 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.01–2.5 mL/h in 0.01 mL/h increments; 0.01–0.09 mL/h available only with 1 mL and 3 mL syringes |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual covering the 8015 PC Unit, 8100 Pump Module, and 8110 Syringe Module, plus supporting documentation for the two infusion modules. Verify installed software, facility Data Set, administration-set compatibility, approved syringe compatibility, and individual system configuration before clinical use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Medley Pump Module 8100 Series Directions for Use
Download PDF
Alaris Syringe Module v9 Quick Reference Guide
Download PDF
In stock
$3,185.00
Fully Refurbished
1-Year Warranty
Biomed Tested & Calibrated
Complete Working System
- Includes 1× Alaris 8015 PC Unit + 1× Alaris 8100 LVP Pump Module + 1× Alaris 8110 Syringe Module
- Two infusion modalities — large-volume and syringe infusion — managed through one PC Unit
- Guardrails Suite MX compatible • wireless-capable PC Unit • expandable modular Alaris platform
Alaris Medley Combo #2
Refurbished • 1-Year Warranty • Alaris 8015 PC Unit with one 8100 large-volume channel and one 8110 syringe-infusion channel
The Alaris Medley Combo #2 combines one Alaris 8015 PC Unit , one Alaris 8100 Pump Module , and one Alaris 8110 Syringe Module . The PC Unit provides the common system interface, while the 8100 delivers large-volume infusions and the 8110 provides syringe-based infusion capability. This combination gives facilities two different infusion modalities on the same modular Alaris platform.
What’s Included
- 1× CareFusion Alaris PC Unit, Model 8015 — system controller and programming interface
- 1× CareFusion Alaris Pump Module, Model 8100 — single-channel large-volume infusion module
- 1× CareFusion Alaris Syringe Module, Model 8110 — precision syringe infusion module
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, Alaris Medley Combo #2 combines large-volume and syringe infusion capabilities through a single Alaris 8015 PC Unit. The PC Unit supplies the common programming interface, power, and communications connection for both attached infusion modules.
The 8100 Pump Module supports continuous or intermittent large-volume delivery of fluids, medications, blood, and blood products. The 8110 Syringe Module provides continuous or intermittent syringe-based delivery for adult, pediatric, and neonatal patients. When used with an appropriately configured Alaris System, Guardrails Suite MX can apply facility-defined Profiles, Drug Library entries, dosing limits, and Clinical Advisories.
- One 8015 controller with one large-volume and one syringe-infusion channel
- 8100 flow rate: 0.1–999 mL/h • VTBI: 0.1–9999 mL
- 8110 flow rate: 0.01–999 mL/h depending on syringe size • approved syringe sizes span 1–60 mL
- Guardrails Suite MX compatible when an appropriate facility Data Set is installed
- Wireless-capable PC Unit; wireless functionality depends on installed hardware, software, network configuration, and facility settings
- Compatible administration sets, approved syringes, and appropriate facility configuration are required for clinical use
Specifications — Alaris 8015 PC Unit
| Manufacturer | CareFusion / BD |
| Model | 8015 — Alaris PC Unit |
| Type | System controller and common programming interface for compatible Alaris infusion and monitoring modules |
| Display | 4.7-inch diagonal display; display presentation may vary with facility Data Set and system configuration |
| Dimensions | 6.9″ W × 8.8″ H × 9″ D, including pole clamp |
| Weight | 7.2 lb |
| Module Capacity | Maximum of four infusion or monitoring modules; an Auto-ID Module may be included as a fifth module |
| Battery Operation | Battery runtime varies with module count and activity; manufacturer reference specifies approximately 6 hours with one Pump Module infusing at 25 mL/h using a new, fully charged battery |
| AC Power | 100–240 V AC, 50/60 Hz, 150 VA maximum |
| Communication Data Port | RS-232 with RJ45 connector |
| Safety Software | Compatible with Guardrails Suite MX; available Profiles, Drug Libraries, limits, and features depend on the installed facility Data Set and system configuration |
| Connectivity | Wireless-capable; wireless operation depends on installed hardware, software, network configuration, and facility settings |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–85% noncondensing for the 4.7-inch small-screen PC Unit |
| Software | Installed software version may vary by refurbished unit; verify the individual PC Unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8100 Pump Module
| Manufacturer | CareFusion / BD |
| Model | 8100 — Alaris Pump Module |
| Type | Single-channel large-volume infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Delivery | Continuous or intermittent infusion |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.6 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h |
| Flow-Rate Programming Increments | 0.1 mL/h from 0.1–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Volume to Be Infused (VTBI) | 0.1–9999 mL |
| VTBI Programming Increments | 0.01 mL from 0.1–9.99 mL; 0.1 mL from 10–999.9 mL; 1 mL from 1000–9999 mL |
| Rate Accuracy | ±5% at 1–999 mL/h and ±5.5% below 1 mL/h under manufacturer-specified test conditions |
| Occlusion — Pump Mode | 525 mmHg at rates of 30 mL/h or greater; threshold varies with rate and patient back-pressure below 30 mL/h |
| Occlusion — Selectable Mode | User-selectable from 50–525 mmHg in 25 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.1–20 mL/h in 0.1 mL/h increments |
| Air-in-Line Detection | Ultrasonic air-in-line detection |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8110 Syringe Module
| Manufacturer | CareFusion / BD |
| Model | 8110 — Alaris Syringe Module |
| Type | Syringe infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Administration Routes | Clinically acceptable routes including intravenous, intra-arterial, subcutaneous, epidural, enteral, and irrigation of fluid spaces |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D |
| Weight | 4.5 lb |
| Operating Principle | Positive displacement |
| Overall Flow Rate Range | 0.01–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.01–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Syringe-Specific Flow Ranges | 50/60 mL: 0.1–999 • 30 mL: 0.1–650 • 20 mL: 0.1–500 • 10 mL: 0.1–250 • 5 mL: 0.1–150 • 3 mL: 0.01–100 • 1 mL: 0.01–30 mL/h |
| Volume to Be Infused (VTBI) | 0.1–60 mL |
| Rate Accuracy | ±2% of full-scale plunger travel, excluding syringe variation |
| Syringe Compatibility | Approved syringe sizes span 1–60 mL. Compatible manufacturer and model combinations depend on installed Syringe Module software, country-specific compatibility documentation, and approved system configuration. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available selection list; the displayed syringe manufacturer/type and size must be verified before use |
| Maximum Infusion Pressure | Approximately 800 mmHg without pressure-sensing disc; 1060 mmHg with pressure-sensing disc |
| Occlusion Alarm Threshold | Without pressure-sensing disc: Low, Medium, or High; with pressure-sensing disc: user-selectable 25–1000 mmHg in 1 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.01–2.5 mL/h in 0.01 mL/h increments; 0.01–0.09 mL/h available only with 1 mL and 3 mL syringes |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual covering the 8015 PC Unit, 8100 Pump Module, and 8110 Syringe Module, plus supporting documentation for the two infusion modules. Verify installed software, facility Data Set, administration-set compatibility, approved syringe compatibility, and individual system configuration before clinical use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Medley Pump Module 8100 Series Directions for Use
Download PDF
Alaris Syringe Module v9 Quick Reference Guide
Download PDF
- Includes 1× Alaris 8015 PC Unit + 1× Alaris 8100 LVP Pump Module + 1× Alaris 8110 Syringe Module
- Two infusion modalities — large-volume and syringe infusion — managed through one PC Unit
- Guardrails Suite MX compatible • wireless-capable PC Unit • expandable modular Alaris platform
Alaris Medley Combo #2
Refurbished • 1-Year Warranty • Alaris 8015 PC Unit with one 8100 large-volume channel and one 8110 syringe-infusion channel
The Alaris Medley Combo #2 combines one Alaris 8015 PC Unit , one Alaris 8100 Pump Module , and one Alaris 8110 Syringe Module . The PC Unit provides the common system interface, while the 8100 delivers large-volume infusions and the 8110 provides syringe-based infusion capability. This combination gives facilities two different infusion modalities on the same modular Alaris platform.
What’s Included
- 1× CareFusion Alaris PC Unit, Model 8015 — system controller and programming interface
- 1× CareFusion Alaris Pump Module, Model 8100 — single-channel large-volume infusion module
- 1× CareFusion Alaris Syringe Module, Model 8110 — precision syringe infusion module
Product Description
Fully refurbished and backed by a 1-year United Infusion warranty, Alaris Medley Combo #2 combines large-volume and syringe infusion capabilities through a single Alaris 8015 PC Unit. The PC Unit supplies the common programming interface, power, and communications connection for both attached infusion modules.
The 8100 Pump Module supports continuous or intermittent large-volume delivery of fluids, medications, blood, and blood products. The 8110 Syringe Module provides continuous or intermittent syringe-based delivery for adult, pediatric, and neonatal patients. When used with an appropriately configured Alaris System, Guardrails Suite MX can apply facility-defined Profiles, Drug Library entries, dosing limits, and Clinical Advisories.
- One 8015 controller with one large-volume and one syringe-infusion channel
- 8100 flow rate: 0.1–999 mL/h • VTBI: 0.1–9999 mL
- 8110 flow rate: 0.01–999 mL/h depending on syringe size • approved syringe sizes span 1–60 mL
- Guardrails Suite MX compatible when an appropriate facility Data Set is installed
- Wireless-capable PC Unit; wireless functionality depends on installed hardware, software, network configuration, and facility settings
- Compatible administration sets, approved syringes, and appropriate facility configuration are required for clinical use
Specifications — Alaris 8015 PC Unit
| Manufacturer | CareFusion / BD |
| Model | 8015 — Alaris PC Unit |
| Type | System controller and common programming interface for compatible Alaris infusion and monitoring modules |
| Display | 4.7-inch diagonal display; display presentation may vary with facility Data Set and system configuration |
| Dimensions | 6.9″ W × 8.8″ H × 9″ D, including pole clamp |
| Weight | 7.2 lb |
| Module Capacity | Maximum of four infusion or monitoring modules; an Auto-ID Module may be included as a fifth module |
| Battery Operation | Battery runtime varies with module count and activity; manufacturer reference specifies approximately 6 hours with one Pump Module infusing at 25 mL/h using a new, fully charged battery |
| AC Power | 100–240 V AC, 50/60 Hz, 150 VA maximum |
| Communication Data Port | RS-232 with RJ45 connector |
| Safety Software | Compatible with Guardrails Suite MX; available Profiles, Drug Libraries, limits, and features depend on the installed facility Data Set and system configuration |
| Connectivity | Wireless-capable; wireless operation depends on installed hardware, software, network configuration, and facility settings |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–85% noncondensing for the 4.7-inch small-screen PC Unit |
| Software | Installed software version may vary by refurbished unit; verify the individual PC Unit before clinical use |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8100 Pump Module
| Manufacturer | CareFusion / BD |
| Model | 8100 — Alaris Pump Module |
| Type | Single-channel large-volume infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Delivery | Continuous or intermittent infusion |
| Dimensions | 3.3″ W × 8.9″ H × 5.5″ D (8.4 × 22.6 × 14 cm) |
| Weight | 2.6 lb |
| Operating Principle | Positive displacement |
| Flow Rate Range | 0.1–999 mL/h |
| Flow-Rate Programming Increments | 0.1 mL/h from 0.1–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Volume to Be Infused (VTBI) | 0.1–9999 mL |
| VTBI Programming Increments | 0.01 mL from 0.1–9.99 mL; 0.1 mL from 10–999.9 mL; 1 mL from 1000–9999 mL |
| Rate Accuracy | ±5% at 1–999 mL/h and ±5.5% below 1 mL/h under manufacturer-specified test conditions |
| Occlusion — Pump Mode | 525 mmHg at rates of 30 mL/h or greater; threshold varies with rate and patient back-pressure below 30 mL/h |
| Occlusion — Selectable Mode | User-selectable from 50–525 mmHg in 25 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.1–20 mL/h in 0.1 mL/h increments |
| Air-in-Line Detection | Ultrasonic air-in-line detection |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof patient-applied part |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Specifications — Alaris 8110 Syringe Module
| Manufacturer | CareFusion / BD |
| Model | 8110 — Alaris Syringe Module |
| Type | Syringe infusion pump module |
| System Requirement | Requires a compatible Alaris PC Unit; does not operate as a standalone infusion pump |
| Patient Population | Adult, pediatric, and neonatal patients |
| Infusion Applications | Fluids, medications, blood, and blood products |
| Administration Routes | Clinically acceptable routes including intravenous, intra-arterial, subcutaneous, epidural, enteral, and irrigation of fluid spaces |
| Dimensions | 4.5″ W × 15.0″ H × 7.5″ D |
| Weight | 4.5 lb |
| Operating Principle | Positive displacement |
| Overall Flow Rate Range | 0.01–999 mL/h, subject to syringe-size restrictions |
| Flow-Rate Programming Increments | 0.01 mL/h from 0.01–9.99 mL/h; 0.1 mL/h from 10–99.9 mL/h; 1 mL/h from 100–999 mL/h |
| Syringe-Specific Flow Ranges | 50/60 mL: 0.1–999 • 30 mL: 0.1–650 • 20 mL: 0.1–500 • 10 mL: 0.1–250 • 5 mL: 0.1–150 • 3 mL: 0.01–100 • 1 mL: 0.01–30 mL/h |
| Volume to Be Infused (VTBI) | 0.1–60 mL |
| Rate Accuracy | ±2% of full-scale plunger travel, excluding syringe variation |
| Syringe Compatibility | Approved syringe sizes span 1–60 mL. Compatible manufacturer and model combinations depend on installed Syringe Module software, country-specific compatibility documentation, and approved system configuration. |
| Automatic Syringe Identification | Automatically detects syringe size and narrows the available selection list; the displayed syringe manufacturer/type and size must be verified before use |
| Maximum Infusion Pressure | Approximately 800 mmHg without pressure-sensing disc; 1060 mmHg with pressure-sensing disc |
| Occlusion Alarm Threshold | Without pressure-sensing disc: Low, Medium, or High; with pressure-sensing disc: user-selectable 25–1000 mmHg in 1 mmHg increments |
| KVO Default | 1 mL/h when programmed rate is 1 mL/h or above; programmed rate when rate is 0.9 mL/h or below |
| KVO Configurable Range | 0.01–2.5 mL/h in 0.01 mL/h increments; 0.01–0.09 mL/h available only with 1 mL and 3 mL syringes |
| Fluid Ingress Protection | IPX2 — Drip Proof |
| Shock Protection | Type CF, Defibrillator Proof |
| Operating Temperature | 41–104°F (5–40°C) |
| Operating Relative Humidity | 20–90% noncondensing |
| Storage / Transport Temperature | -4–140°F (-20–60°C) |
| Storage / Transport Relative Humidity | 5–90% noncondensing |
| Condition | Refurbished |
| Warranty | 1-Year United Infusion warranty |
Product Manuals
Download the CareFusion Alaris System User Manual covering the 8015 PC Unit, 8100 Pump Module, and 8110 Syringe Module, plus supporting documentation for the two infusion modules. Verify installed software, facility Data Set, administration-set compatibility, approved syringe compatibility, and individual system configuration before clinical use.
Alaris System User Manual — PC Unit Model 8015, Software v9.33
Download PDF
Medley Pump Module 8100 Series Directions for Use
Download PDF
Alaris Syringe Module v9 Quick Reference Guide
Download PDF
Refurbishing Process
At United Infusion, we follow a comprehensive refurbishing process for infusion pumps to help ensure they operate safely and reliably. This process follows manufacturer guidelines and sanitation standards to meet high quality expectations.
Below are the key steps of our refurbishing process:
2. Disassembly
The pump is carefully disassembled to access internal components, including the motor, gears, tubing pathways, and electronics. All parts are handled with care to avoid added damage.
3. Cleaning & Sanitization
Appropriate disinfectants are used to thoroughly clean all parts and remove residual fluids, blood, or debris. This step follows sanitation standards to help ensure the device is free from contaminants.
4. Component Inspection & Replacement
Individual parts, including the motor, battery, display screen, buttons, and connectors, are inspected for wear, damage, or malfunction. Worn or damaged components are replaced with manufacturer-approved parts.
5. Calibration & Software Update
The pump is adjusted to support accurate fluid delivery rates using standardized testing methods, and calibration is verified against manufacturer specifications. The latest compatible software version is then installed to improve functionality.
6. Testing, Reassembly & Final Check
The pump goes through functional testing, including alarms, flow rate accuracy, occlusion detection, and bolus delivery. It is then reassembled, connections are checked, and a final visual and functional inspection is completed to confirm it meets safety standards and customer requirements.
"We needed our syringe pumps serviced for scheduled maintenance to continue to provide safe care. In the past, we had to send them off with a 6 weeks turn around time. Then we found United Infusion. 30 min down the road, 24 hr turn around and 30 minutes down the road. We are extremely grateful!!!"
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